Tag | Content |
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EnhancerAtlas ID | HS055-00814 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:230889730-230891080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr1:230889862-230889872 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:230889885-230889895 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr1:230889883-230889898 | AAGGGGCGGGGCTTC | - | 6.3 | SP2 | MA0516.2 | chr1:230889882-230889899 | GAAGGGGCGGGGCTTCC | - | 6.26 | SP4 | MA0685.1 | chr1:230889881-230889898 | GGAAGGGGCGGGGCTTC | - | 6.66 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_32194 | chr1:230887396-230890088 | Gastric | SE_32194 | chr1:230890338-230891556 | Gastric | SE_33557 | chr1:230879014-230891230 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I230750 | chr1 | 230885992 | 230891172 |
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Enhancer Sequence | TTATGGTTTG TCTCTTCCTC AAATGCAATT TGCAAAACTC TCCTGAACGA AACAACAGCT 60 TCTGGGAGGT GGTGGCAGCT GCAGGCACAG TGGGCGCCGT GGGTGAGGCC AGGGCTGAGG 120 CAGGCTGGGG GAGGGGCGGG GCAGGAGGCT GGGAAGGGGC GGGGCTTCCG AGAGCACCGC 180 CCTCCGCGTC CAGGGCAGCT CCACCAGGGC AGGGGCTTTC CCTCTCTCTT TGTTGTCGTC 240 CAATGTCAGG AATGGAGCCC AGCAACTCAA AGAGTGGAAG AATATATGCA TATCATAAGA 300 TTGCTTTCTA CACTTTTTTG TTCATGTTTT ATAAATACCC CTCCATATTG TATATGTATA 360 TATTAATATG TATTAATGAT TACATTAATA CACATAGTGT ATGTGCTTAT GTGTAATATA 420 GAATAATATA TATATAATGC ACTTCGGTGA AACAATATGA GAGATGTGTG CATATCTCTC 480 TTTATATGGT ATAGATACAT GAAATTTTAC CTAAGCGCAT CTCTGTAAAA AGAAACACTG 540 AGCAGGGTGG CATGTGTCTG TAACCTCAAT ACCTTGGGAA TCCAAGGCGG GAGGATCACT 600 TGAGGCCAGG AGTTTGAGAC CAGCCTGGGC AACATAGCGA GACCCCCATC TCCACAAAAA 660 AAAAAAAAAA AAAATTAAAA AGTGGCTGGG CGTGGTGACT CACGTCTGTA GTCCCAGTTA 720 CTTGGGAGGC TGAGGTGGAA GGATTGCTTG AGCCCAGAAG GTCAAGGCTG TAGTGAGCTA 780 TGATCATGTC ACTGCACTCC AGCCTGGGTG ACACAGCAAG ATTCTGTCTC TAAACCTATA 840 TATATTTGGA ATCCACTTTG TGGGGGAAGG ATTATATAAA GAAAGAAATG GAGAAGCTGG 900 GTGGGTAGGG AGTATGTTTA GTCCAAGGCC CCAGCCTGTG GTACATGCAT TACTCAGCTC 960 CTTGAAGCCC ACAGAGGTCA CAGAGCTCAC AGCTGGGATA GCCCTGGACT CCTAGCCCAG 1020 TGCCTGAGTG AGCACAGGAA TCCTCAGTGT GTGGCTGATG TCCAGCTTTG TGGCCGGGTG 1080 TGGCCTGTGT TTCTGGCCAG AGATTGGTGC TGAGTGCAGC TCAGGAGGCA GGACCTCTCC 1140 CCGGCGGAGG AGATTTACCA AAGATGAGCC CAGCCTTATC CAGAGCATAG AGAGGTGGCA 1200 GCCTTTTACA TCCACGTGGC CCTCCTCAGG GAAAAGAATC AAGCACAGGG AAAGCCCTCT 1260 GCCCCAAGAA AGCAGAGAGA CCCTGAGCCT ACCCTTTCAT AGTGGCTTGC AGCATGGCAG 1320 GCCTCAGCCT AATAACACTC TCATTCCTCC 1350
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